Prevalence of Class 1 Integrons and Extended Spectrum Beta Lactamases among Multi-Drug Resistant Escherichia coli Isolates from North of Iran

Background: Extended spectrum beta lactamases (ESBLs) are an important cause of transferable multidrug resistance (MDR) in gram-negative bacteria. The most described ESBL genes are generally found within integron-like structures as mobile genetic elements. The aim of this study was to identify the accompanying of class 1 integrons and ESBLs in the MDR E. coli isolates. Methods: Susceptibility to antimicrobial agents was determined for 33 E. coli strains by the disk diffusion method. Double-disk synergy test was applied for screening ESBL. To identify the strains carrying integrons, the conserved regions of integron-encoded integrase gene intI1 were amplified. For detection of gene cassettes, 5′CS and 3′CS primers were used. Results: All E. coli isolates were identified as multi-drug resistant. More than 50% of the isolates were resistant to tetracycline, cephalothin, cefuroxime, amoxicillin-clavulanic acid, and third generation cephalosporines. Nearly all of the isolates displayed sensitivity to piperacillin. There was a significant correlation between production of ESBL and resistance to all antibiotics except for ciprofloxacin and piperacillin (P < 0.01). Thirty two MDR strains (97%) included class 1 integron, and some isolates that included integrons were similar in the size of gene cassettes. The isolates were different in the resistance profiles; however, some others had similar resistance profiles. Of eight ESBL positive isolates, seven (87.5%) carried class 1 integrons. Conclusion: Class 1 integrons were frequent in MDR and also ESBL-producing E. coli isolates. High prevalence of class 1 integrons confirms that integron-mediated antimicrobial gene cassettes are important in E. coli resistance profile.


INTRODUCTION
espite accessibility to different antibiotics, Urinary tract infections (UTIs) are the second most frequent community-acquired adult infection and the main cause of nosocomial infection [1]. E. coli is one of the major causes of nosocomial infections, especially in patients in intensive care units and the main cause of UTI in developed world, accounting for 70-90% of uncomplicated UTIs [2].
Understanding the molecular mechanism of resistance genes may help to the introduction of new antimicrobial strategies and some preventive procedures to prevent further spreading of resistance determinants among the pathogens [3]. Several resistance genes encode different mechanisms of drug resistance in bacterial genomes and in extra-chromosomal pieces of DNA [4].
Multidrug resistance (MDR) is a major problem worldwide and encoded by resistance genes exists on integrons. Integrons are mobile genetic elements considered to be responsible for the MDR transfer. Most of the integrons reported in clinical isolates are class 1 inegrons. Class 1 integrons carry integrase gene (intI1), which codes for the site-specific recombinase responsible for cassette insertion [5,6]. Integrase gene also includes the attI1 site, where the cassettes are integrated and a promoter, Pc, is responsible for the transcription of the cassette-encoded genes [5,7]. Gene cassette contains a single antibiotic resistance gene and a 59-base element (or attC site) downstream of the gene, which is responsible for recombination events [8].
Extended spectrum beta lactamases (ESBLs) are a D group of enzymes that are common among Enterobacteriaceae [9]. They are the increasingly important cause of transferable MDR in Gram-negative bacteria throughout the world. ESBLs also have the ability to hydrolyze third and fourth generation cephalosporins and monobactams. ESBL-producing strains are prevented by lactamase inhibitors (clavulanic acid, sulbactam, and tazobactam) [10]. ESBL-encoding genes are generally located on conjugative plasmids (such as blaTEM or blaSHV), although many of the most newly described ESBL genes are usually found within integron-like structures (such as blaCTX-M, blaGES, or blaVEB-1) [11][12][13]. On the other hand, ESBL-producing isolates usually show resistance to other antibiotics including aminoglycsides, tetracyclines, chloramphenicol, trimethoprim, sulfonamides, or quinolones. Resistance to these antibiotics is mostly related to presence of different resistance genes on plasmids, transposons, or integrons as transferable elements or genetic structures generated by combinatorial evolution of different interactive pieces [13][14][15]. The presence of ESBL genes on integrons can facilitate the distribution of such genetic elements [11,12].
The aim of this study was to identify whether there are mechanisms of resistance in the E. coli isolates causing UTIs from north of Iran or not.

Sample collection and identification of bacterial strains.
Urine samples were collected from appropriate patients in early morning mid-stream using sterile, wide mouthed glass bottles with screw cap tops between May and July 2012. Samples were maintained in an icebox until laboratory analysis. It did not last more than one hour between sample collection and sample analysis. Urine samples were cultured on nutrient, blood and MacConkey agar plates and incubated at 37°C for 18-24 h. The usual bacteriological methods were applied for cultivation, isolation and identification of isolates from urine samples. The isolates were stored at -70ºC in a tryptic soy broth containing 15% glycerol until processing. The isolates were entitled as E1 to E33.

Phenotypic detection of ESBLs.
Double-disk synergy tests were performed by placing disks of ceftazidime, cefotaxime, and cefepime (30 μg each) at 30 or 20 mm distance (center to center) from a disk containing amoxicillin (20 μg) and clavulanic acid (10 μg). When the cephalosporin zone was expanded by the clavulanate, ESBL production was supposed. It means that the zones produced by the disks with clavulanate were ≥5 mm larger than those without any inhibitor [16].

Detection of class 1 integrons by PCR.
The existence of class 1 integrons was identified by PCR using specific primers for the integron integrase genes intI1 (Table 1). A single colony of each isolate was suspended in 25 ml reaction mixture containing 2.5 ml 10× PCR, 1.5 ml 50 mM MgCl 2 , 2 ml 2.5 mM dNTP, 1 ml primer (forward and reverse) together with 1 unit Taq DNA polymerase (5 U/ml). Volume of the reaction mixture was adjusted by adding filtered deionized water. PCR assays were performed in a DNA thermal cycler (BioRad, USA). The PCR conditions were initial denaturation at 94ºC for 12 min, followed by 30 cycles of 1 min at 94ºC, 30 s at 60ºC for annealing, 2 min at 72ºC for elongation, and final extension was conducted at 72°C for 10 min. A reagent blank was included in every PCR assay containing all components of the reaction mixture except for the bacteria. ATCC E. coli 25922 strain was used as negative control for all PCR assays, and E. coli ur-31 was used as positive control for intI1 gene. PCR products were subjected to horizontal gel electrophoresis on 1% agarose gel (type II, Sigma, USA) in Tris-borate EDTA buffer at 100 volt (50 mA) at room temperature for 1 h. DNA bands were visualized by gel staining with ethidiumbromide (0.5 mg/ml) for 30 min and then photographed [17]. Detection of gene cassettes. To characterize the gene cassettes inserted in the class 1 integrons, the fragments including the cassette regions were amplified by PCR. The primers used to amplify cassettes of class 1 integrons were 5ĆS and 3ĆS (Table  1) as mentioned previously [18].

RESULTS
Antimicrobial resistance. The resistance patterns of the 33 urinary isolates are shown in the Table 2. All E. coli isolates (33 strains) were identified as multi-drug resistant. More than 50% of the isolates were resistant to tetracycline, cephalothin, cefuroxime, amoxicillinclavulanic acid, and third generation cephalosporines. Nearly all isolates displayed sensitivity to piperacillin.

Detection of class 1 integrons and gene cassettes.
PCR analysis revealed that 32 strains (97%) contained IntI1 gene (Fig. 1). Among the eight ESBL-producing strains, seven had class 1 integrons. The detected fragment size was 483 bp. The strains including integrons had variable gene cassettes (Fig. 2). One or maximum four gene cassettes was carried by class 1 integrons. Based on PCR amplification with primers 5ĆS and 3ĆS, the inserted gene cassettes of class 1 integrons were identified as 100, 250, 500, and 700 bp. The isolates similar in the number of gene cassettes were compared based on the results of disk diffusion (Table 3). Some isolates were similar in the size of gene cassettes, which seemed that they were different in the resistance profiles; however, some other had similar resistance profiles.

DISSCUSION
Multi-drug resistant bacteria have been recently a problem in hospitalized patients worldwide. The frequency of MDR among clinical isolates is highly variable throughout the world and in different geographic areas and is rapidly changing according to time [19]. MDRs encoded by linked resistance genes exist on integrons, which are potentially movable genetic elements supposed to be involved in transferring MDR. This study was designed to examine the drug resistance pattern, the frequency of the class 1 integrons and ESBLs among the MDR E. coli isolates in UTI patients in north of Iran, Rasht.
Based on the results, E. coli was the most frequent microorganism isolated from urine samples. Other investigators also reported that E. coli was the most commonly isolated aerobic microorganism from UTIs [20,21]. In our study, similar to Salem et al. survey [17], all E. coli isolates were recognized as MDR. In Ahangarzadeh Rezaee et al. study [22], 84.2% of the isolates were multi-drug resistant.
Nearly all E. coli isolates in this survey were sensitive to piperacillin, while some of them were resistant to other antimicrobials. The isolates displayed variable patterns of resistance to different antibiotics. More than 50% of the isolates were resistant to tetracycline, cephalothin, cefuroxime, amoxicillinclavulanic acid, and third generation cephalosporines. According to Salem et al. [17], all E. coli isolates displayed resistance to penicillins, amoxicillin, cephalexin, and chloramphenicol. The isolates showed variable patterns of resistance to tetracycline, sulfamethoxazole-trimethoprim, erythromycin, and quinolone group.
The antimicrobial resistance genes located on integron-like structures are being dramatically reported worldwide [11]. Most of the newly described ESBL genes are generally found within integron-like structures (such as blaCTX-M, blaGES, or blaVEB-1) [11,13]. On the other hand, ESBL-producing isolates are usually resistant to other antibiotics, such as aminoglycosides, tetracyclines, chloramphenicol etc. The fact that ESBL genes could be acquired by strains including particular integrons enlarges the possibilities of the selection of these strains by a variety of different antimicrobials. In addition, ESBL genes can be located on integrons, which may simplify the distribution of such genetic elements [11,12]. For detection of class 1 integrons and ESBLs in this study, PCR amplification of intI1 gene and Doubledisk synergy test method were used, respectively. Based on the results, 97% and 24% of the isolates contained class 1 integrons (483 bp in size) and ESBLs, respectively, which is indicative of very high frequency of occurrence of class 1 integrons in E. coli strains. Also, nearly all ESBL isolates carried class 1 integrons.
The presence of class 1 and class 2 integrons were also investigated in Salem et al. study [17]. The results indicated that the class 1 integrons were observed in E. coli isolates (54%), and IntI1 gene yielded a DNA fragment of 1900 bp upon amplification by PCR, but class 2 integrons showed negative results. The absence of IntI2 gene may be attributed that class 2 integrons found in 4 to 20% uropathogenic E. coli strains [24,25] as well as in other human pathogens [26], other animal pathogens [27], and various commensal bacteria [28,29]. Essen-Zandbergen et al. [30], reported that among all E. coli isolated from animals, class 1 integrons were found in 76%, and the size of gene cassettes were 600, 1000, 1550, 2000, 2200, and 2500 bp. Martinez-Freijo et al. [31] study represented that 62% of E. coli isolates were integron 1-positive and had different sizes of inserted gene cassette, including 1500, 1600, 1800, 2000, and 3000 bp. In Farshad et al. [32] study performed in Shiraz (Iran), of 96 E. coli isolates from urine samples tested, 6.25% of the strains were the integron 1-positive isolates. In other words, the prevalence of class 1 integrons among the isolates was low.
In Madrid (Spain), Machado et al. [33] investigated the existence of class 1 integrons in ESBL-producing in 133 E. coli isolates and reported that 39% of the isolates were ESBL producing, and class 1 integrons were more common among 67% of the isolates. Thus, based on their study, a significant relationship was not observed between the spread of genetic elements encoding ESBL and the dispersion of integrons in these isolates.
Karimi et al. [34] detected class 1 integrons in ESBL producing in 100 E. coli isolates in Tehran, Iran. Thirty E. coli isolates were positive for ESBLs, and the frequency of class 1 integrons was 52%. Also, 54% of ESBL producers had class 1 integrons. The detected fragment of intI1 was 9000 bp.
In a survey by Al-Assil et al. [35] in Aleppo (Syria), 61.33% of uropathogenic E. coli were ESBL producers, and class 1 integrons were detected in 54.6% of them. Prevalence of class 1 integrons in ESBL isolates was 34%.
In conclusion, this study demonstrates that unlike other researches, the prevalence of class 1 integrons in ESBL producing E. coli strains is very common. The results of the current study also indicated that there are at least two resistance mechanisms in our isolates, and they can be transferred to other clinical strains, then it is very important to identify and control the resistant strains. Increased resistance may be related to the lack of proper research, abuse of chemotherapeutic agents, public misuse of antibiotics, and little or no preventive measure. Thus, piperacillin can be used as a therapeutic agent or the most effective antibiotic in controlling UTI infections in the patients infected by ESB-producing E. coli carrying class 1 integrons in Rasht (Guilan Province, Iran). Nevertheless, more studies are needed to be performed in this area.